5.1    Introduction

A fundamental property of living organisms is their ability to reproduce. Bacteria and fungi can divide to produce daughter cells that are identical to the parental cells. Sexually reproducing organisms produce offspring that are similar to themselves.

On a cellular level, this reproduction occurs by mitosis, the process by which a single parental cell divides to produce two identical daughter cells.

Meiosis is the process in which cells with a diploid genome produce four germ cells (haploid cells). Regardless of the type of cell division, the duplication of all of the genetic material is needed so that each daughter cell receives a full complement of genetic material.

In this chapter, we look at the details of replication as well as differences in detail between prokaryotic and eukaryotic replication that arise because of differences in DNA packing.

We will begin with a discussion on the general features of replication common to the replication of ‘naked’ prokaryotic DNA and of chromatin-encased eukaryotic DNA, arisen early in the evolution of replication biochemistry.

You will read about experiments that explored or revealed answers to some basic questions like:

1. Where does replication begin? Is it one region on the chromosome or several?
2. Is the start random or at a specific location?
3. Once replication begins in which direction does replication occur?

Answers to many of these questions arose from experiments carried out in E. coli, which has a circular genome.

We will then introduce all the proteins involved in carrying out this essential process to develop a complete picture of how DNA replication occurs, ending with differences between prokaryotic and eukaryotic replication that arise because of differences in DNA packing.

5.2  The Basic Rules of Replication

DNA Replication is essential for life and as a process, it must be

1. Accurate (make few mistakes)
2. Fast
3. Complete (although we will see one exception when it comes to the ends of linear chromosomes.)

It takes an army of proteins and some specialized DNA sequences that function together to accomplish this!

While the individual components are important, it is important to not lose sight of some general principles of replication that are common to all of life.

5.2.1 DNA Replication is always semiconservative: Meselson and Stahl Experiments

Watson and Crick’s double helix model suggested a replication mechanism. In presenting the complementary pairing of bases in the double helix, Watson and Crick immediately realized that the base sequence of one strand of DNA can be used as a template to make a new complementary strand.

This was the semi-conservative model of replication. However, how DNA can separate (denature) was not understood and there were alternative models of replication (Figure 5.1)

Conservative Model: Perhaps there is some DNA synthesizing machine in the cell that can take dsDNA and make a copy of it?

Dispersive Model: Perhaps the process of replication could break the parental DNA into pieces and use them to seed the synthesis of new DNA.

It was far from obvious what the mechanism would be. However, these three models make different predictions about the behavior of the two strands of the parental DNA during replication.

Meselson and Stahl set out to test the three possible models of replication and confirmed that DNA replication is semi-conservative. (Due to the simplicity and indisputable results of the experiment, the Meselson-Stahl experiment has been called “the most beautiful experiment in biology.” see Link to Learning)

In their experiment, E. coli cells were grown in a medium containing ¹⁵N, a ‘heavy’ nitrogen isotope.  After many generations, all of the DNA in the cells had become labeled with the heavy isotope.   At that point, the ¹⁵N-tagged cells were placed back in a medium containing the more common, ‘light’ 14N isotope and allowed to grow for exactly one generation.

Fig. 5.2 (below) shows Meselson and Stahl’s predictions for their experiment.  Meselson and Stahl knew that ¹⁴N-labeled and ¹⁵N-labeled DNA would form separate bands after centrifugation on CsCl chloride density gradients.

They tested their predictions by purifying and centrifuging the DNA from the ¹⁵N-labeled cells grown in ¹⁴N medium for one generation.

They found that this DNA formed a single band with a density between that of ¹⁵N-labeled DNA and ¹⁴N-labeled DNA, eliminating the conservative model of DNA replication (possibility #1).

That left two possibilities: replication was either semiconservative (possibility #2) or dispersive (possibility #3).

The dispersive model was eliminated when DNA isolated from cells grown for a 2nd generation on ¹⁴N were shown to contain two bands of DNA on the CsCl density gradients.

5.2.2  DNA Replication Begins at Specific Chromosomal Sites

Where does replication begin? Does the DNA unwind at one region on the genome or in multiple places? Is it random or are there special sequences on the DNA where the process of unwinding begins?

The answers to some of the fundamental questions came from the direct visualization of bacterial DNA using a technique called autoradiography– an imaging technique utilizing radioactive sources contained within the exposed sample.

Cairns Experiment

In 1963, John Cairns cultured E. coli cells for long periods on ³H-thymidine (³H-T) to make all of their cellular DNA radioactive.  He then extracted the DNA (during replication) and allowed it to adhere to membranes.

A sensitive film was placed over the membrane and time was allowed for the radiation to expose the X-ray film. As the radioactive substance decays the emissions create a pattern on the x-ray film. When the film is developed an image of the pattern is seen, similar to the light that exposes a photographic film. The image obtained is an autoradiograph.

The image pictured in Figure 5.3 shows dark lines (tracks of silver grains in the autoradiographs) that reveal the pattern of replicating DNA molecules.

Cairns called these replicating chromosomes theta images because they resembled the Greek letter theta (θ).

From his many autoradiographs, he arranged a sequence of his images to illustrate his inference that replication starts at a single origin of replication on the bacterial chromosome, proceeding around the circle to completion.

5.2.3 Most DNA Replication Is Bidirectional

The theta images obtained above do not distinguish between uni-directional or bi-directional replication forms of replication for the bacterial chromosome.

In Uni-directional replication-  a new DNA molecule is synthesized in one direction only. DNA unwinds at ONE replication fork and moves around the entire circular DNA until complete.

In Bi-directional replication- there are 2 growing points, DNA unwinds, and new DNA is synthesized at BOTH replication forks until they meet at the opposite end from where replication began (the origin).

Additional experiments demonstrated that DNA replication is bi-directional.

• Cells were labeled with ³H-thymidine with low specific activity to lightly label the replication bubble.
• Then the cells were labeled with a much stronger radioactive isotope for a short time.
• Any newly synthesized DNA would be labeled with a stronger label and appear darker on the images.
• Visualization of chromosomes revealed darker segments on BOTH ends of the replication bubble.

Conclusion: Replication indeed begins at one location of the origin of replication, generating a replication bubble, and DNA at both ends of the bubble unwinds in opposite directions, replicating DNA both ways away from the origin at the replication forks.

5.2.4   DNA Polymerase Catalyzes Phosphodiester-Linkage Formation

Before we consider what happens at replication forks in detail, let’s focus our attention on DNA POLYMERASES- a class of enzymes that catalyze the step-wise addition of nucleotides to a DNA strand.

Most of our information on DNA replication mechanisms and machinery comes from prokaryotic systems like E. Coli.  In Bacteria there are five different DNA polymerases indicated by Roman numerals I, II, III, IV, and V. Of these the ones of most interest to us are DNA Polymerase III and DNA Polymerase I.

Chemistry of DNA Synthesis

All DNA Polymerase enzymes have some common properties:

1. It requires all four dNTPs as well as Mg 2+ ions.
2. DNA polymerase is a template-directed enzyme. The polymerase will only make the phosphodiester bond efficiently when there is a match with a base on the template strand. DNA Polymerases are therefore often called DNA Dependent DNA Polymerase  (they need a DNA template to make more DNA!)

BUT

3. All DNA polymerases discovered to date can only elongate a preexisting DNA or RNA strand called a Primer. They cannot initiate chains!

DNA polymerase catalyzes the reaction by which an incoming deoxyribonucleotide, complementary to the template, is added onto the 3′ end of the previous nucleotide. The importance of the 3’OH group lies in the reaction that builds a chain of nucleotides.

The reaction catalyzed by the DNA polymerase occurs through the nucleophilic attack by the 3’OH group of the last nucleotide of the growing strand on the α phosphate of the incoming dNTP (Figure 5.4). The 5′ phosphate of the new nucleotide binds to the 3′ OH group of the nucleotide to make a phosphodiester bond.

The immediate hydrolysis of the pyrophosphate that is cleaved off the incoming dNTP drives the reaction forward.

Each added nucleotide provides a new 3’OH, allowing the chain to be extended for as long as the DNA polymerase continues to synthesize the new strand.

Thus DNA synthesis always occurs in the 5′ to 3′ direction. Scientists have yet to identify a polymerase that can add bases to the 5′ ends of DNA strands.

4. Lastly all polymerases can correct mistakes! They have two different active sites, one for synthesizing and a separate  3′-5′ EXONUCLEASE activity, which we shall see shortly.

Some polymerases like DNA pol I also have an additional 5′-3′ exonuclease activity, the significance of which will become apparent later!

Primer Synthesis

If DNA polymerases can only extend a 3’OH group, how does DNA synthesis ever get started? How is this primer made?

Solution: RNA polymerases make the same type of bond (phosphodiester), however unlike DNA polymerases they do not require a preexisting base-paired 3′ end to initiate synthesis.

In the cell, an enzyme, called Primase assembles a short stretch of RNA – the PRIMER base paired to the parental DNA template. Given the similarity between RNA and DNA, DNA polymerases can extend the free 3′ OH group provided by RNA!

Thus DNA synthesis begins with first synthesizing a little RNA!

The PRIMER-TEMPLATE junction is the cellular substrate recognized by DNA polymerase.

Primase is a  slow (relatively!) and error-prone polymerase. The error-prone nature of its activity is not a problem, because the cell will remove all the RNA primers later in the process of DNA synthesis and replace them with DNA nucleotides- and we’ll revisit this later in this reading.

5.2.5 DNA synthesis at the replication fork semi-discontinuous

Consider one replication fork shown below. Here the DNA strands of separated, and the DNA ahead of the fork remains wound in a double helix. The separated strands serve as templates for new daughter strand synthesis. Remember this fork is moving- the downstream DNA is continuously being unwound and upstream DNA is continuously being replicated into hybrid helices of old and new DNA strands.

Recall that the newly synthesized DNA must also be anti-parallel to the parental DNA!

When we look at the diagram it will appear as though both the new strands are being made in the same direction! But that would violate one of the fundamental rules of nucleic acid chemistry- that synthesis can only occur in the 5′-3′ direction.

This conundrum is solved, by copying DNA continuously on one template strand and discontinuously on the other.

One template strand is oriented such that the 5’-to-3’ direction in which the daughter strand synthesis can take place in the direction of fork movement continuously. This is known as the LEADING STRAND.

DNA copied from the other template strand, on the other hand, is made in short segments away from the fork or discontinuously.

Each of these fragments begins with an RNA primer (dark blue in the diagram above) which is extended by DNA polymerase. This strand of DNA is known as LAGGING STRAND.  The short stretches of DNA generated during lagging strand synthesis are commonly known as Okazaki fragments after their discoverer Reiji Okazaki. In bacteria, Okazaki fragments are 1,000-2,000 nucleotides in length, whereas in the cells of higher organisms, they are typically only 100-200 nucleotides long.

Eventually, these short segments of DNA will have to be stitched together by an enzyme called DNA LIGASE.

Note that Lagging strand synthesis still takes place in a 5’-to-3’ direction and no rules of nucleic chemistry are violated. 

See here for an animation of this process: Animation of Bidirectional-Semidiscontinous Replication (YouTube)

5.3 DNA Polymerases- Structure

The three-dimensional structures of several DNA polymerase enzymes are known.

The shape has been compared to that of a hand (or baseball mitt) with the protein domains referred to as the fingers, the thumb, and the palm. (see diagram on right )

Each subdomain carries a specific function. The finger domain binds the incoming dNTP, the thumb domain helps grip duplex DNA, and the palm domain contains the amino acids that are part of the active site of the enzyme. The catalytic palm domain is the most conserved of the domains.

 5.3.1 Accuracy of Replication

Changes in DNA sequence (mutations) can change the amino acid sequence of the encoded proteins and can often (though not always!) be harmful to the functioning of the organism.

When billions of bases in DNA are copied during replication, how do cells ensure that the newly synthesized DNA is a faithful copy of the original information?

DNA synthesis is extremely accurate with only one error per 10⁹ bases!

3 Mechanisms contribute to the remarkable accuracy of replication

1. The change in the structure of the enzyme when it binds the correct nucleotide. The DNA polymerase clasps the ds DNA tightly before binding the new dNTP.  Within the active site of a DNA polymerase, the incoming dNTP is tested. A perfect fit triggers a conformational change: the finger domain rotates to form a tight pocket into which only a properly shaped base pair will readily fit.

Recall that the complementary base pairing (A with T and G with C) results in just the correct width for DNA!

The proper base is favored by the formation of a base pair, which is stabilized by specific hydrogen bonds. The binding of a non-complementary base is less likely because the interactions are energetically weaker.

2. 3′-5′ Exonucleolytic Proofreading: Recall that DNA polymerases can correct mistakes in DNA by removing mismatched nucleotides. This happens using the 3′-5′ EXONUCLEASE activity that allows it to snip out the incorrect base replace it with the correct base and resume replicating the template strand.

3. Strand Directed Mismatch Repair:  A special mechanism inside cells to correct mismatches that have already been incorporated. We will learn about mismatch repair in the DNA Repair unit!

Before you continue you should

Complete any exercises and watch associated lecture videos

5.4 Process of Replication

Our understanding of the process of DNA replication is derived from studies using bacteria, yeast, and other systems. These investigations have revealed that DNA replication is carried out by the action of a large number of proteins that act together as a complex protein machine. (Table 5.1) This complex machine is known as REPLISOME.

Although the specific proteins involved are different in bacteria and eukaryotes, the basic mechanisms and principles are relevant in all cells.

We will primarily describe the process as discovered in Prokaryotes and point out differences with Eukaryotes towards the end.

5.4.1 Stages of Replication

As with many processes in molecular biology, we conventionally look at replication as being made up of three phases – initiation, elongation, and termination.

5.4.1 Stage 1: Initiation of Replication

As we have seen, DNA synthesis starts at one or more origins or replication. How does the replication machinery know where to begin?

Origins are specific nucleotide sequences where replication begins. In E. coli (as do most prokaryotes), there is a single origin of replication (ori-C) on its one chromosome. This region is depicted in Figure 5.6

Figure 5.6. Schematic of the architecture of E. coli origin oriC. Diagram by S. Mehta (CC-BY-SA)

The region includes:

•  Several conserved sequences which serve as binding sites for  a protein called DnaA [DnaA boxes]
• An AT-rich region also called the DNA Unwinding Element
• GATC Methylation sites. (not shown in Figure above)

A-T base pairs have two hydrogen bonds between them and are more readily disrupted than G-C base pairs which have three. Therefore DNA with a sequence of repetitive A-Ts can easily ‘open up’.

Initiation of replication begins when INITIATOR PROTEINS (DnaA for E. coli) will recognize and bind to the sequences present within the origins of replication.

For E.coli

• The initiator protein is called – DnaA.  Dna A recognizes and binds to the DnaA- sequences (green boxes above).
• The binding of these proteins promotes the recruitment of multiple DnaA subunits that form a helical oligomer
• Bending of the DNA and torsional stress promotes the melting of the adjacent DNA unwinding element (AT- rich region)
• This process usually needs ATP

Unwinding

Once a small region of the DNA is opened up at each origin of replication, the DNA helix must be unwound to allow replication to proceed.

How are the strands of the parental DNA double helix separated?

The unwinding of the DNA helix requires the action of a class of enzymes called HELICASES.

Helicases are motor proteins that move (at speeds up to that of a jet engine!) directionally along a nucleic acid phosphodiester backbone, separating two annealed nucleic acid strands such as DNA and RNA, using energy from ATP hydrolysis.

Helicase loads onto the lagging strand and is a ring-shaped protein.

Note that a replication bubble is made up of two replication forks that “move” or open up, in opposite directions. At each replication fork, the parental DNA strands must be unwound to expose new sections of the single-stranded template.

[In E.coli the loading of the helicase is a two-step process but let’s not complicate things!]

Two problems arise as a result of unwinding DNA

1. The separated single strands of DNA must be kept from coming back together so the new strands can continue to be synthesized.

Solution: To ensure that unwound regions of the parental DNA remain single-stranded and available for copying, the separated strands of the parental DNA are quickly coated by many molecules of a protein called single-strand DNA binding protein. (SSB)

2. A knotty problem: What is the effect of unwinding one region of the double helix? The local unwinding of the double helix causes over-winding (increased positive supercoiling) ahead of the unwound region. The DNA ahead of the replication fork has to rotate, or it will get twisted on itself and halt replication. This is a major problem, not only for circular bacterial chromosomes but also for linear eukaryotic chromosomes, which, in principle, could rotate to relieve the stress caused by the increased supercoiling.

Solution: Topoisomerases

Topoisomerases are special enzymes that can relieve the topological stress caused by the local “unwinding” of the extra winds of the double helix. They do this by cutting one or both strands of the DNA and allowing the strands to swivel around each other to release the tension before rejoining the ends.

In E. coli, the topoisomerase that performs this function is called DNA GYRASE.

DNA gyrase moves ahead of the replication fork and is essential for the process of replication.

Watch this animation to better understand the concept of supercoiling

Loading Primase

What’s next? Remember DNA polymerases cannot begin synthesis of a new DNA strand. They need a free 3′ OH to which they can add DNA nucleotides.

The helicase recruits primase which synthesizes RNA primers used to initiate DNA synthesis.

5.4.2 DNA Replication Machine

Once the RNA primer is established it can be extended by DNA polymerase enzymes. DNA polymerase III is the main polymerase involved in both leading strand biosynthesis and the synthesis of the Okazaki Fragments during DNA replication.

The polymerases are part of a large replication machine that consists of many different proteins organized in a structure known as the Holoenzyme. (Figure 5.7)

A cartoon of the arrangement is shown on the right in the diagram below.

It includes 3 units of  [the glove-like structures (in black) in the cartoon]  of DNA Pol-III catalytic core attached to a central component via flexible linker proteins. The central component contains proteins (green and red) that together make up the Sliding Clamp loader and Sliding clamp.

Role of Sliding Clamp and Clamp Loader

Consider that the chromosome of E. coli consists of almost five million base pairs. Because DNA replication in E. coli takes place simultaneously from two replication forks, the overall rate of DNA synthesis is 1,600 nucleotides per second. Thus, E. coli is capable of duplicating its entire chromosome in as little as 40 minutes, and as we will see below, it does so with considerable accuracy.

This property of remaining attached to the DNA through many rounds of nucleotide addition is referred to as processivity. Processivity maximizes the speed of DNA synthesis.

If the polymerase frequently fell off the DNA and had to re-bind to resume nucleotide incorporation, the rate of DNA synthesis would be much slower.

This is where the sliding clamp and clamp loader come in.

The shape of the clamp  – a ring-shaped structure provides a geometrically elegant and simple solution.

DNA polymerases are tethered to the DNA by a sliding clamp, which (being ring-shaped) fully encircles the DNA helix.

Sliding clamps cannot load onto DNA spontaneously because they are closed circles.  The job of the clamp loader is to ‘load’ the clamp onto the DNA.

When the primer is formed, Adenosine triphosphate (ATP)–dependent clamp loaders open the sliding clamps and load them onto primer-template junctions.

Hydrolysis of ATP to ADP then changes the affinity of the clamp loader for the clamp and leaves it behind. The clamp spontaneously closes encircling the DNA helix.  (Figure 5.8).

The sliding clamp is then joined by the DNA Polymerase in front.

In the presence of the sliding clamp, DNA polymerases are much more processive, making replication faster and more efficient.

Once the sliding clamp and DNA pol III cores are engaged the process of elongation begins!

Before you continue you should list/order the events that have taken place in Initiation thus far.

5.4.3 Stage 2: Elongation of Replication

During elongation, the core polymerase (glove part of DNA pol III) adds DNA nucleotides to the 3′ ends of the newly synthesized polynucleotide strand. The template strand specifies which of the four DNA nucleotides (A, T, C, or G) is added at each position along the new chain. Only the nucleotide complementary to the template nucleotide at that position is added to the new strand.

Co-ordination of Leading and Lagging Strand Synthesis

Lagging synthesis is straightforward, as the DNA Polymerase can keep extending behind the moving machinery in the direction of unwinding.

Recall, however, that the lagging strand (chemistry) necessitates synthesizing in short fragments in a direction away from the moving replication fork, yet the polymerases are tethered to the clamp loader as part of one big machinery.

Examining the composition of the holoenzyme, notice that there are three units of polymerase. One of the units of DNA polymerase is engaged in leasing strand synthesis. The other two move back and forth to generate okazaki fragments and carry out leading strand synthesis.

The lagging template strand loops around so that the synthesis of DNA in the 5′-3 direction can take place in the direction of the moving replication fork. One core-polymerase engages with the looped Okazaki fragment. It begins extension and the DNA is released as helicase proceeds forward.

As the core polymerase continues to extend the Okazaki fragment a newly primed section is formed at the replication fork, which is then captured by the third polymerase. This mode of replication has been termed the trombone model because the size of the loop lengthens and shortens like the slide on a trombone! (See animation below)

This looping allows the primase and the Pol III active site to accomplish the discontinuous synthesis of the lagging template strand even though the general direction of the Pol III complex is opposite to the required direction of DNA synthesis.

The DNA Replication Animation below highlights the whole process:

Completing Elongation

Eventually, the RNA primers need to be removed and one long continuous DNA strand needs to be made.

Removal of RNA primer nucleotides from Okazaki fragments requires the action of DNA polymerase I.

In addition to DNA synthesizing (5′-3), and proofreading (3′-5 exonuclease), DNA polymerase I also has a 5′ → 3′ exonuclease activity.

DNA Pol I binds to the gap between the end of an Okazaki fragment and the RNA primer that marks the beginning of the next Okazaki fragment.

Using its 5′-3′ exonuclease activity DNA pol I removes the ribonucleotide from RNA primer. This creates a gap opposite the template which can be filled in with correct deoxyribonucleotide (dNTP) using the 5′-3 polymerase capability. DNA Pol-I continues in this manner until the RNA primer is replaced.

In the end, a small gap “nick” exists between adjacent Okazaki fragments. This gap is sealed or ‘ligated’ using the enzyme  DNA ligase, which catalyzes  the final phospho-diester bond (Figure 5.9)

5.4.4 Stage 3: Termination of Prokaryotic Replication

Proper termination of DNA replication is important for genome stability. E. coli replication terminates in the region opposite oriC.

The two replication forks meet at a termination region, setting off a series of events that lead to the eventual completion of replication and subsequent chromosome separation.

The termination region contains special conserved sequences called  (Ter) sites. These sequences are recognized by Tus proteins.

The 10 Ter sites are split and organized as two oppositely orientated groups of five. The association of the Tus proteins to the Ter sites is also polar, such that there is a permissive face that allows the replisome to pass unhindered and a non-permissive face that can block the replisome (Figure 5.9).

This configuration allows the replisome to pass the first Tus-Ter complex unhindered and be blocked at the second. When the 2 replisomes meet the apparatus disassembles.

We now have 2 circular chromosomes that are linked to one another.

Here the activity of a different enzyme from the Topisomerase family becomes useful in separating or unlinking the 2 chromosomes.

Before you continue you should

1. Watch the Lecture videos that cover the material above.

5.5 Eukaryotic Replication

Replication in eukaryotes while mechanistically similar to replication in bacteria is more challenging in the following ways.

1) Size: E. coli must replicate 4.6 million base pairs, whereas a human diploid cell must replicate 6 billion base pairs.

2) While the genetic information for E. coli is contained on one chromosome, human beings have 23 pairs of chromosomes that must be replicated.

3) While the E. coli chromosome is circular, human chromosomes are linear. The third challenge arises because of the nature of DNA synthesis on the lagging strand. Linear chromosomes are subject to shortening with each round of replication unless countermeasures are taken.

4) The events of replication have an additional twist in eukaryotes. Recall that DNA is found in eukaryotic cells as chromatin, a complex of the DNA with proteins. The nucleosome structure must be disrupted to make DNA available for replication and restored after replication is completed.

The solution to Challenges 1 and 2 :

Origin organization, specification, and activation in eukaryotes are more complex than in bacterial or archaeal kingdoms and significantly deviate from the paradigm established for prokaryotic replication initiation.

To account for replicating large genome sizes – eukaryotic chromosomes have multiple origins of replication, which are located between 30 and 300 kilobase pairs (kbp) apart.

In human beings, replication of the entire genome requires about 30,000 origins of replication, with each chromosome containing several hundred.

Each origin of replication represents a replication unit or replicon, and at each origin, replication is semi-discontinuous and bi-directional.

The essential steps of replication are the same as in prokaryotes:

Before replication can start, the DNA has to be made available as a template.

– A helicase using the energy from ATP hydrolysis opens up the DNA helix.

– Replication forks are formed at each replication origin as the DNA unwinds.

– The opening of the double helix causes over-winding, or supercoiling, in the DNA ahead of the replication fork. These are resolved with the action of topoisomerases.
– Primers are formed.

The differences often are in the number of proteins needed for these functions.

For example:

1. The eukaryotic origin sequences are recognized by a large complex of proteins called the  Origin Recognition Complex, instead of a single protein.

2. The number of DNA polymerases in eukaryotes is more than those found in prokaryotes: 14 are known, of which five are known to have major roles during replication and have been well studied. They are known as pol α, pol β, pol γ, pol δ, and pol ε.

At the eukaryotic replication fork, three distinct replicative polymerase complexes contribute to DNA replication: α, δ, and ε.

3. The primers for DNA synthesis are hybrid and consist of RNA+ DNA. The enzyme responsible for priming is DNA polymerase α (Pol α) – This protein has 2 parts- one which synthesizes DNA (not unlike all the DNA polymerases) the other has RNA priming activity.

Thus this complex accomplishes the priming task by synthesizing a primer that contains a short ~10-nucleotide RNA stretch followed by 10 to 20 DNA bases.

Importantly, this priming action occurs at the origins to begin leading-strand synthesis and also at the 5′ end of each Okazaki fragment on the lagging strand.

However, Pol α is not able to continue DNA replication– it is not processive!

4. After priming, synthesis is  “handed off” to 2 other polymerases to continue elongation. The polymerase switching requires clamp loaders and is unique to eukaryotes.

5. The polymerase switching or handoff occurs to two different DNA polymerases – one for the leading strand DNA pol δ, and for the lagging strand to DNA pol ε.

5.5.1 Dealing with Histones

As seen in Chapter 4 chromosomes are packaged by wrapping ~147 nucleotides (at intervals averaging 200 nucleotides) around an octamer of histone proteins, forming the nucleosome. The histone octamer includes two copies each of histone H2A, H2B, H3, and H4.

It was highlighted that histone proteins are subject to a variety of post-translational modifications, including phosphorylation, acetylation, methylation, and ubiquitination that represent vital epigenetic marks.

The nucleosome structure must be disrupted to make DNA available for replication and restored after replication is completed.

Furthermore, it is important to transmit the epigenetic information found on the parental nucleosomes to the daughter nucleosomes, in order to preserve the same chromatin state.

In other words, the same histone modifications should be present on the daughter nucleosomes as were on the parental nucleosomes. This must all be done while doubling the amount of chromatin, which requires the incorporation of newly synthesized histone proteins.

This process is accomplished by histone chaperones and chromatin remodeling complexes.

Ahead of the replication fork, the chromatin structure is disassembled by ATP-dependent chromatin remodeling complexes, allowing access to the DNA template. The loss of the histone octamer from the parental DNA during DNA replication is accompanied by the dissociation of H3/H4  tetramers and  H2A/H2B dimers.

Special histone protein chaperones recruit histone H3-H4 dimers to the replication fork- helping load both newly synthesized (light purple) histones to establish chromatin behind the fork. Previously loaded histones (dark purple) are also deposited on both daughter DNA strands.

Thus in the reassembled chromatin, half of the histones are recycled from the parental chromatin while the other half are newly synthesized.

(Figure 5.12)

The presence of some recycled histones allows for one possible mechanism of how the epigenetic state is re-established. Presumably, the old histones would still be carrying the modifications (acetyl or methyl groups for example) which can then facilitate the spread of modifications using Bromo and Chromodomain-containing complexes that have histone-modifying activity.

For example, old histone bearing an acetyl group is recognized by a bromodomain-containing Histone acetyl Transferase, which will then acetylate adjacent histones.

Scientists are still uncovering how this important aspect of ‘somatic’ cell identity is maintained.

5.5.2 End Replication Problem- Replicating Telomeres

As you’ve learned, the enzyme DNA polymerase can add nucleotides only in the 5′ to 3′ direction. Leading strand synthesis continues until the end of the chromosome is reached. On the lagging strand, DNA is synthesized in short stretches, each of which is initiated by a separate primer.

When the replication fork reaches the end of the linear chromosome, there is no way to replace the primer on the 5’ end of the lagging strand leaving a structure called a 3’-overhang or a 5’-gap (Fig 5.13).

Interestingly, this overhang is critically important in forming a ‘cap-like structure at the end of the chromosome called the telomere.

Telomeres are a highly repetitive noncoding sequence at the 3′ ends that are recognized by proteins that bind the DNA sequence and packed into a compact T-loop structure that hides the ends of the chromosomes. This structure is important because it hides the ends of chromosomes and prevents DNA repair machinery from mistaking chromosomal ends for double-stranded DNA breaks.

Essentially it tells the cell “Hey, I’m the normal end of the chromosome- leave me alone; don’t try and fix me!” 

If the shortening at the ends of the chromosomes was not fixed, eventually the highly repetitive sequence of the telomere would be lost and the cap structure at the ends of the chromosomes would no longer form, causing the cell to signal that the DNA was damaged.

To combat the loss of DNA sequence in the telomere and prevent a DNA damage response, an enzyme called telomerase (Figure 5.13), adds nucleotides to the ends of chromosomes.

Telomerase is highly expressed in early development and gametic cells; it is moderately expressed in many adult stem cells, but not expressed in most adult somatic cells.

Telomerase is an enzyme that contains a catalytic part and a built-in RNA template. Because it uses an RNA template to build DNA (transcription in reverse), it is called reverse transcriptase.

Telomerase attaches to the 3’-overhang (location of a 3’OH group) and adds extra repeats (DNA nucleotides). It does this by using the RNA component as a template. 

Once the 3′ end of the template is sufficiently elongated, there is room for primase to lay down new primers that will be extended by DNA polymerase. After this is complete and the final RNA primer is removed, the short stretch of single-stranded DNA (the 3’-overhang) will regenerate the cap structure of telomeres.

 

 

In many cancer cell types, the expression of the telomerase activity has been reactivated, allowing cancer cells to lengthen telomeres and become immortal.

Because of this action, there is great interest in better understanding how telomerase and the telomere are regulated in cells and if there are ways to exogenously control the enzyme.

Dr. Mehta Lecture Video: L211 Eukaryotic Replication Playlist

Link to Learning

This You-Tube Video compares the process of prokaryotic and eukaryotic replication

References and Attributions

This chapter contains material taken from the following CC-licensed content. Changes include rewording, removing paragraphs and replacing with original material, and combining material from the sources.

1. Bergtrom, Gerald, “Cell and Molecular Biology 4e: What We Know and How We Found Out” (2020). Cell and Molecular Biology 4e: What We Know and How We Found Out – All Versions. 13.
   https://dc.uwm.edu/biosci_facbooks_bergtrom/13
2. Works contributed to LibreTexts by Kevin Ahern and Indira Rajagopal. LibreTexts content is licensed by CC BY-NC-SA 3.0
3. Fundamentals of Cell Biology by Shoshana D. Katzman, et al., Georgia Gwinnet College, licensed by Attribution-NonCommercial-ShareAlike 4.0 (available https://alg.manifoldapp.org/projects/fundamentals-of-cell-biology)

Figure image attributions are provided within the text.

D. Samson, L. H. John F. Cairns (1922–2018). Nat Struct Mol Biol 26, 149–150 (2019). https://doi.org/10.1038/s41594-019-0194-1. See here:  https://rdcu.be/crdJs